Clinical Data & Systems Intern
Confidential
Posted: February 3, 2026
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Quick Summary
We are seeking a Clinical Data & Systems Intern to join our team in Coyol, Alajuela, Costa Rica. The ideal candidate will have experience in clinical data management and systems, with a strong background in medical devices and a passion for innovation.
Required Skills
Job Description
About Us:
Establishment Labs is changing the medical device, breast health, aesthetics and reconstruction industry by designing, developing, and manufacturing an innovative portfolio of advanced medical aesthetic device technologies and wellness solutions. It is currently the world’s fastest-growing women’s health company.
Our Femtech solutions are proudly produced at two MDSAP-certified, carbon neutral, LEED Gold certified, state-of-the-art manufacturing facilities in Costa Rica and are approved for sale in more than 85 countries.
Since 2018 the company trades on the NASDAQ stock exchange under the ticker symbol ESTA and has a market cap of around $1.8 billion.
This is an exciting opportunity to join an innovative international company in hyper-growth as we launch a significant revolution to transform the women´s aesthetics industry.
Main activities:
Support clinical data science/management and systems activities for global clinical investigations.
Perform tasks such as:
Data entry
Data cleaning
Reconciliation support
Oversight of essential documents
Use validated platforms, including:
Electronic Data Capture (EDC)
Electronic Trial Master File (eTMF)
Participate in:
Data tracking
Query management workflows
Documentation quality control
Apply:
Protocol requirements
Data management plans
Good Clinical Practice (GCP) standards
Contribute to the Clinical Data and Systems workgroup by supporting:
Internal reports and study metrics
Operational tools and system documentation
Reference materials to enhance data quality and workflow efficiency
Ensure audit readiness and regulatory compliance
Collaborate with:
Clinical Study Managers
Clinical Research Associates (CRAs)
External vendors
Support the Global Clinical Medical and Regulatory Affairs divisions with both study-specific and broader initiatives
Aim to ensure:
High-quality data collection
Efficient study execution across global regions
Develop core competencies in:
Clinical data science/management
Documentation oversight
Digital systems operations within a GCP-governed environment
Requirements:
Must be pursuing (e.g., Biology, Pharmacy, Biotech, Medicine, Biochemistry) or related fields such as Statistics, Informatics, or Biomedical Engineering.
Fluent English (written, spoken) B2+
Required Skills:
Teamwork
Organization
Active listening
Ability to understand what is being requested
Analytical skills and the ability to express oneself clearly
Problem-solving and troubleshooting skills
Open to collaborating with other departaments
Strong commitment
Data manipulation and analysis (Excel, Python/R ideal)
Important Details:
Minimum 4 days per week, flexibility to adjust working hours based on university.
On Site Internship: Coyol Free Zone, Alajuela
The company will provide a financial subsidy
The contract will last a minimum of 6 months to a maximum of 11 months.